Bispecific antibody complex pre-targeting and targeted delivery of polymer drug conjugates for imaging and therapy in dual human mammary cancer xenografts

2014 ◽  
Vol 41 (8) ◽  
pp. 1603-1616 ◽  
Author(s):  
Ban-An Khaw ◽  
Keyur S. Gada ◽  
Vishwesh Patil ◽  
Rajiv Panwar ◽  
Savitri Mandapati ◽  
...  
2012 ◽  
Vol 2 (1) ◽  
pp. 65-76 ◽  
Author(s):  
Keyur S. Gada ◽  
Vishwesh Patil ◽  
Rajiv Panwar ◽  
Arash Hatefi ◽  
Ban-An Khaw

2011 ◽  
Vol 32 (12) ◽  
pp. 1231-1240 ◽  
Author(s):  
Keyur S. Gada ◽  
Vishwesh Patil ◽  
Rajiv Panwar ◽  
Stan Majewski ◽  
Yared Tekabe ◽  
...  

2020 ◽  
Vol 11 (45) ◽  
pp. 7137-7146
Author(s):  
Mehmet Arslan ◽  
Burcu Sumer Bolu ◽  
Rana Sanyal ◽  
Amitav Sanyal

Increasing interest in utilization of polymeric systems in targeted drug delivery has necessitated fabrication of polymers that undergo facile functionalization with targeting groups and therapeutic agents in a modular and orthogonal fashion.


2015 ◽  
Vol 24 (6) ◽  
pp. 475-491 ◽  
Author(s):  
Minglu Chang ◽  
Fang Zhang ◽  
Ting Wei ◽  
Tiantian Zuo ◽  
Yuanyuan Guan ◽  
...  

2018 ◽  
Author(s):  
James Leighton ◽  
Linda M. Suen ◽  
Makeda A. Tekle-Smith ◽  
Kevin S. Williamson ◽  
Joshua R. Infantine ◽  
...  

With an average GI50 value against the NCI panel of 60 human cancer cell lines of 0.12 nM, spongistatin 1 is among the most potent anti-proliferative agents ever discovered rendering it an attractive candidate for development as a payload for antibody-drug conjugates and other targeted delivery approaches. It is unavailable from natural sources and its size and complex stereostructure render chemical synthesis highly time- and resource-intensive, however, and its development requires more efficient and step-economical synthetic access. Using novel and uniquely enabling direct complex fragment coupling alkallyl- and crotylsilylation reactions, we have developed a 22-step synthesis of a rationally designed D-ring modified analog of spongistatin 1 that is equipotent with the natural product, and have used that synthesis to establish that the C(15) acetate may be replaced with a linker functional group-bearing ester with only minimal reductions in potency.<br><div><br></div>


2019 ◽  
Vol 18 (15) ◽  
pp. 2078-2092 ◽  
Author(s):  
Mala Sharma ◽  
Chitranshu Pandey ◽  
Neha Sharma ◽  
Mohammad A. Kamal ◽  
Usman Sayeed ◽  
...  

Background: Nanotechnology pictures a breakthrough in the domain of cancer therapy owing to its novel properties and functions. This technology is quite amendable as it allows the scientists to engineer drug nanoparticles of dimensions 10nm – 500nm permitting them to pass via leaky vasculature of tumorigenic microenvironment with higher specificity, reduced cytotoxicity and effective release without any after effects. The central part of the review zooms onto the role of nanoparticles and their targeted delivery for the cure of cancer. Methods: The novel and various versatile nanoparticle platforms viz. polymeric (drug-conjugates, micelles, dendrimers), Lipid-based (liposomes, solid nanoparticle, nanostructured lipid carrier, lipid-polymer hybrid), and stimuli-sensitive (thermoresponsive, ultrasound, pH-responsive, hydrogel) etc. have been designed for a persistent, précised nanodrug delivery and the co-delivery of collegial drug conjugates leading to the formation of safer release of myriad of drugs for cancer chemoprevention. Results: The review concerns about tracing and detailing the drug delivery systems of cancer nanotechnology. Conclusion: Nanotechnology is bestowed with the design, depiction, fabrication, and application of nanostructures, and devices with their controlled delivery together with the imaging of the selected target site and drug release at the specific site of action.


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